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dbVar

Database of genomic structural variation

nsv5642784

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Ebert et al. 2021

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 93 SVs from 22 studies. See in: genome view

Submitted genomic172,076,255-172,076,255

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5642784	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	172,076,255	172,076,255
nsv5642784	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	171,503,259	171,503,259

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17138206	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17138206	Submitted genomic		NC_000005.10:g.172 076255_172076256in s171	GRCh38 (hg38)		NC_000005.10	Chr5	172,076,255	172,076,255
nssv17138206	Remapped	Perfect	NC_000005.9:g.1715 03259_171503260ins 171	GRCh37.p13	First Pass	NC_000005.9	Chr5	171,503,259	171,503,259

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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